Charcot Marie Tooth Disease - CMT Disease - Hereditary Neuropathy
THE FOUNDATION TO SUPPORT THOSE LIVING WITH CMT (CHARCOT-MARIE-TOOTH)
"This year, tens of thousands of children will sit on the sidelines because they have CMT. Please join me in supporting HNF and getting them back in the game."
Susan Lucci
Susan Lucci
MEMBER LOGIN
Hereditary Neuropathy Foundation, Inc.
1751 2nd Avenue, Suite 103, NY NY 10128
NY Tel: 212-722-8396
Toll Free: 877-463-1287
info@hnf-cure.org
1751 2nd Avenue, Suite 103, NY NY 10128
NY Tel: 212-722-8396
Toll Free: 877-463-1287
info@hnf-cure.org
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| RESEARCH | ARTICLES | DONATE NOW! |
|---|---|---|
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HNF develops TRIAD Program
Encourages cutting-edge research and addresses needs of CMT people.
read more... 
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Linda Here!
Some people write their biography. Being a writer and an artist, I twisted myself inside out for several years trying to figure out how I could tell the story of my life with CMT in words and pictures.
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| CMT GUIDES | GET CONNECTED | NEWS & EVENTS |
Become a member and receive these essential guides with resources and information that can help.
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Connect with families, friends and caregivers for information and support. click here
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Susan Kinney, an artist with CMT, launches fundraiser for research!
Through her art, Susan Kinney is living proof that you do not have to allow CMT to define you. Read more to find out where to buy her art and support CMT research! |
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